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Doxepin Hydrochloride - 63629-3199-4 - (doxepin hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 63629-3199
Proprietary Name: Doxepin Hydrochloride
Non Proprietary Name: doxepin hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   doxepin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Doxepin Hydrochloride

Product NDC: 63629-3199
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070791
Marketing Category: ANDA
Start Marketing Date: 20110504

Package Information of Doxepin Hydrochloride

Package NDC: 63629-3199-4
Package Description: 120 CAPSULE in 1 BOTTLE (63629-3199-4)

NDC Information of Doxepin Hydrochloride

NDC Code 63629-3199-4
Proprietary Name Doxepin Hydrochloride
Package Description 120 CAPSULE in 1 BOTTLE (63629-3199-4)
Product NDC 63629-3199
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxepin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110504
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name DOXEPIN HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Doxepin Hydrochloride


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